Publication | Open Access
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
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Citations
67
References
2023
Year
Neurodegenerative DiseasesDevelopmental BiologyMendelian DisorderGenetic DisorderMonoallelic VariationGeneticsCharcot-marie-tooth DiseaseMedicineDegenerative DiseaseNeuroscienceDisease Gene IdentificationDexh-box Helicase Dhx9Neurogenetics
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